HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966529Generated: October 30, 2026
Diisobutylamine → 5-(2-Diisobutylamino-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester
https://huagongshe.com/reaction/966529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylamine | HCID 8085 | — |
| Reactant | 5-(2-Methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester | HCID 23393852 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(2-Diisobutylamino-ethyl)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester | HCID 10202333 | 77.5% |
Reaction Steps
To a solution of 5-(2-methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic acid benzyl ester (360 mg, 0.93 mmol, Example 56, Step D) in dioxane (10 mL) was added diisobutylamine (1.62 mL, 9.3 mmol). The mixture was stirred at 100° C. overnight and then partitioned between methylene chloride and water. The organic phase was washed with water and brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo to give a solid residue, which was purified by chromatography (20% ethyl acetate in hexanes) to give 303 mg (77%) of the desired product as a white solid: mp 134-135° C.; MS(APCI+): m/z 421.3 (MH+); Anal. Calcd for C27H36N2O2: C, 77.10; H, 8.63; N, 6.66. Found: C, 76.94; H, 8.75; N, 6.55.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951848B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-d2c47aef91744d27b9933cd9d7213eb3 |
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| Source note | uspto-grants-2005_10 |
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